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rs587779884

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779884(C;T)
Make rs587779884(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position90784953
GeneBLM
is asnp
is mentioned by
dbSNPrs587779884
ebirs587779884
HLIrs587779884
Exacrs587779884
Varsomers587779884
Maprs587779884
PheGenIrs587779884
hapmaprs587779884
1000 genomesrs587779884
hgdprs587779884
ensemblrs587779884
gopubmedrs587779884
geneviewrs587779884
scholarrs587779884
googlers587779884
pharmgkbrs587779884
gwascentralrs587779884
openSNPrs587779884
23andMers587779884
23andMe allrs587779884
SNP Nexus

SNPshotrs587779884
SNPdbers587779884
MSV3drs587779884
GWAS Ctlgrs587779884
Max Magnitude0
ClinVar
Risk rs587779884(T;T)
Alt rs587779884(T;T)
Reference rs587779884(C;C)
Significance Pathogenic
Disease not provided Bloom syndrome
Variation info
Gene BLM
CLNDBN not provided Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91328183C>T
CLNSRC Counsyl
CLNACC RCV000115298.3, RCV000169191.1,